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- Disease Information
- Disease Comparison
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Major Organs-Systems ▼
- Systemic
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Disease Information for Autism/Autistic child
- Clinical Manifestations
- Signs & Symptoms
- Stereotypical Recurrent Attacks
- Apathy/Indifference
- Aphasia
- Delayed speech/language development
- Development Motor Skills (Milestones) Delayed
- Developmental milestones delayed
- Dysphasia
- Hypereactive Child
- Low intelligence/Low IQ
- Mental Deficiency Child
- Mental/motor retardation in children/signs
- Slow Motor Development
- Behavior characteristic/oppositional/rigid/stubborn
- Behavior/obsessive mannerisms
- Bonding to inanimate objects
- Compulsive behavior
- Doesn't Like to be touched/child
- Flat affect
- Idea Fixed/Singleness of thinking
- Interpersonal relationships/absent/flawed
- Pathological lack of Empathy/Others feelings
- Poor bonding in infancy/childhood
- Poor communication skills
- Psychiatric manifestations/problems/difficulties
- Psychomotor retardation
- Resistant to any environment changes
- Ritualistic behavior patterns
- Schizoid personality
- Stereotypy/Repeated movements/activity
- Stress intolerance/emotional
- Stubborn
- Withdrawn Unresponsive
- Macrocephaly/Large head
- Listlessness/lassitude
- Poor Eye contact child/infant
- Disease Progression
- Course/Chronic disorder
- Course/Chronic only
- Demographics & Risk Factors
- Established Disease Population
- Patient/Tuberous sclerosis
- Population Group
- Child
- Population/Pediatrics population
- Sex & Age Groups
- Population/Child
- Population/Child-Infant Only
- Population/Children/all
- Laboratory Tests
- Abnormal Lab Findings (Non Measured)
- Chromosomal abnormality (Lab)
- Neural Growth Factor increased/newborn (Lab)
- Diagnostic Test Results
- Electrodiagnosis
- EEG/Abnormality
- Associated Diseases & Rule outs
- Rule Outs
- Asberger's syndrome
- Attention deficit disorder
- Childhood-onset schizophrenia
- Fragile X retardation syndrome
- Narcolepsy
- Rett's syndrome
- Associated Disease & Complications
- Asperger Syndrome
- Autism
- Infantile autism
- Mental retardation
- Neurodevelopmental disorders
- Psychosis
- Seizure disorder (epilepsy)
- Disease Mechanism & Classification
- Pathophysiology
- Pathophysiology/Gene locus Chromosome 11
- Pathophysiology/Gene locus Chromosome 15
- Pathophysiology/Gene locus Chromosome 16
- Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
- Pathophysiology/Hereditary anticipation/generations worsen
- Pathophysiology/HOXA1 gene mutation
- Pathophysiology/Mitochondrial lesion
- Pathophysiology/Mitochondrial Oxidative sluggish/defect
- Pathophysiology/Neurexin 1 gene deletion
- Process
- PROCESS/Congenital/developmental (category)
- PROCESS/Developmental/delayed expression disorder (ex)
- PROCESS/Hereditary/Genetic predisposition (ex)
- PROCESS/Hereditofamilial (category)
- PROCESS/Psychoses disorder (ex)
- PROCESS/Relational/psychiatric (category)
- Synonyms
- Synonym
- Autism, Autism child, Autism Early Infantile, AUTISM INFANTILE, Autisms, AUTISTIC, autistic disorder, Autistic disorder (disorder), Autistic disorder of childhood onset, Autistic disorder of childhood onset (disorder), autistic disorders, child autism, Childhood autism, disorder autistic, Disorders Autistic, Early Infantile Autism, Infantile Autism, Infantile autism (disorder), Infantile Autism Early, infantile psychosis, Infantile psychosis (disorder), Kanner, Kanner Syndrome, Kanners Syndrome, Kanner's syndrome, psychosis infantile, Syndrome Kanner's, Synonym/Childhood schizophrenia, Synonym/Kanner Syndrome, Synonym/Pervasive developmental disorder/variant
- Definition
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Autism; Infantile Autism; Kanner Syndrome; Autism is a lifelong, nonprogressive neurologic disorder typically appearing before the age of thirty months; It is characterized by language and communication deficits, withdrawal from social contacts and extreme reactions to changes in the immediate environment; About 75 percent of children with autism have low scores on standardized intelligence tests; The outlook for independent living may be improved with intensive training. [NORD 2005]
SNIP genomic markers have been found and there is a gene deletion of neurexin 1; the implication is loss of efficient neuron neuron connection pathophysiology; involved chromosomes are 11 and 15; More common in males 4:1 plus
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- External Links Related to Autism/Autistic child
- Wikipedia
- Merck
- Images
- PubMed (National Library of Medicine)
- NGC (National Guideline Clearinghouse)
- Medscape (eMedicine)
- Harrison's Online (accessmedicine)
- NEJM (The New England Journal of Medicine)